Canonical Allele Identifier: CA2036538862
Gene: KRT5 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516563T= , CM000674.2:g.52516563T= GRCh38
NC_000012.11:g.52910347T= , CM000674.1:g.52910347T= GRCh37
NC_000012.10:g.51196614T= NCBI36
NG_008297.1:g.8897A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1439+74A= MANE Select ENSP00000252242.4:n.1439+74A=
ENST00000252242.8:c.1439+74A= ENSP00000252242.4:n.1439+74A=
ENST00000548409.5:c.561+74A=
ENST00000549511.5:n.646+74A=
ENST00000552629.5:n.1611A=
NM_000424.3:c.1439+74A= NP_000415.2:n.1439+74A=
NM_000424.4:c.1439+74A= MANE Select NP_000415.2:n.1439+74A=
Search 100 bp 5'
Search 100 bp 3'